Evidence map›Paper›PMID 24523507›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Cutaneous T cell lymphoma expresses immunosuppressive CD80 (B7-1) cell surface protein in a STAT5-dependent manner.

Qian Zhang, Hong Yi Wang, Fang Wei, Xiaobin Liu, Jennifer C Paterson, Darshan Roy, Daniela Mihova, Anders Woetmann, Andrzej Ptasznik, Niels Odum and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Role of Tumor Microenvironment in the Pathogenesis of Sézary Syndrome.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Genetics of Cutaneous T Cell Lymphoma: From Bench to Bedside.Current treatment options in oncology · 2016
    Review
  14. A three-signal model of T-cell lymphoma pathogenesis.American journal of hematology · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

Qian ZhangDepartment of Pathology and Laboratory Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19104;
Hong Yi Wang
Fang Wei
Xiaobin Liu
Jennifer C Paterson
Darshan Roy
Daniela Mihova
Anders Woetmann
Andrzej Ptasznik
Niels Odum
Stephen J Schuster
Teresa Marafioti
James L Riley
Mariusz A Wasik
University of Pennsylvania · USUniversity College London · GBUniversity of Copenhagen · DKCedars-Sinai Medical Center · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Novel role of STAT3 in NPM/ALK-induced oncogenesisR01CA096856 · NCI · UNIVERSITY OF PENNSYLVANIA · PI WASIK, MARIUSZ A. · 2002 to 2013
$3.0M
Jak/STAT signaling in human T-cell lymphomasR01CA089194 · NCI · UNIVERSITY OF PENNSYLVANIA · PI WASIK, MARIUSZ A. · 2001 to 2010
$2.5M
Restoring HIV-1 Specific T cell ImmunityR01CA147795 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RILEY, JAMES L. · 2010 to 2014
$1.8M
NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA089194NCI NIH HHS R01 CA096856NCI NIH HHS R01 CA147795NCI NIH HHS R01-CA147795NCI NIH HHS R01-CA89194NCI NIH HHS R01-CA96856
6 · The paper itself

Abstract

In this article, we report that cutaneous T cell lymphoma (CTCL) cells and tissues ubiquitously express the immunosuppressive cell surface protein CD80 (B7-1). CD80 expression in CTCL cells is strictly dependent on the expression of both members of the STAT5 family, STAT5a and STAT5b, as well as their joint ability to transcriptionally activate the CD80 gene. In IL-2-dependent CTCL cells, CD80 expression is induced by the cytokine in a Jak1/3- and STAT5a/b-dependent manner, whereas in the CTCL cells with constitutive STAT5 activation, CD80 expression is also STAT5a/b dependent but is independent of Jak activity. Although depletion of CD80 expression does not affect the proliferation rate and viability of CTCL cells, induced expression of the cell-inhibitory receptor of CD80, CD152 (CTLA-4), impairs growth of the cells. Coculture of CTCL cells with normal T lymphocytes consisting of both CD4(+) and CD8(+) populations or the CD4(+) subset alone, transfected with CD152 mRNA, inhibits proliferation of normal T cells in a CD152- and CD80-dependent manner. These data identify a new mechanism of immune evasion in CTCL and suggest that the CD80-CD152 axis may become a therapeutic target in this type of lymphoma.

Indexed as

AdultB7-1 AntigenBlotting, WesternCell Line, TumorCell ProliferationCells, CulturedCTLA-4 AntigenGene Expression Regulation, NeoplasticHumansImmunohistochemistryInterleukin-2Janus Kinase 1Janus Kinase 3Lymphoma, T-Cell, CutaneousModels, ImmunologicalOligonucleotide Array Sequence AnalysisB7-1 AntigenCTLA-4 AntigenInterleukin-2JAK3 protein, humanJanus Kinase 1Janus Kinase 3STAT5A protein, humanSTAT5B protein, humanSTAT5 Transcription FactorTumor Suppressor Proteins

Identifiers

PMID24523507
PMCPMC3984051
OpenAlexW2115966711

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.